Principal Process Validation Engineer - Pennsylvania, United States

· ←Back to all jobs at VBB · Validation Engineer / Specialist (Southern NJ/Philadelphia) · Validation Engineer / Specialist · Are you hungry to learn, grow, and own your career in · pharmaceutical validation? We're looking for a Validation Engineer / · Specialist who wants hands ...

US WorldMeds is seeking an experienced Quality Validation Engineer in Philadelphia US. · ...

We are seeking the best and the brightest to join our high performing organization as a Project Engineer. · As a leader within the life science industry, we are constantly pushing the boundaries of what is possible and redefining the standards of excellence. ...

· SUMMARY: US WorldMeds is seeking an experienced Quality Validation Engineer to primarily focus on the implementation and validation of equipment, utilities, and systems in the USWM -CT production facility for the manufacture of clinical and commercial GMP pharmaceutical/ biolo ...

Validation Engineer / Specialist · Are you hungry to learn, grow, and own your career in pharmaceutical validation? We're looking for a Validation Engineer / Specialist who wants hands-on experience, regional travel, and a clear path to leadership. · What You'll Do · Support IQ, ...

+ 4+ years of experience in Validation Engineering · + 3+ years of Computer System Validation (CSV) · Experience authorizing and executing validation documents · Hands-on CQV experience including equipment validation temperature mapping ...

US WorldMeds is seeking an experienced Quality Validation Engineer to implement and validate equipment, utilities, and systems in their USWM-CT production facility for clinical and commercial GMP pharmaceutical/biological products. · ...

US WorldMeds seeks Computer System Validation Engineer for compliance and efficiency of computerized systems involved in validation-cycle. · ...

We are seeking a Validation Engineer (CQV – LCMS) to support an industry-leading pharmaceutical organization. · ...

Piper Companies is seeking a Validation Engineer (CQV – LCMS) in Titusville, NJ to support an industry-leading pharmaceutical organization. · ...

Piper Companies seeks Validation Engineer (CQV – LCMS) in Titusville to support pharmaceutical organization. · ...

This role will provide YOU the opportunity to lead key activities to progress YOUR career. · ...

The Senior Validation Engineer is a subject matter expert in the Commissioning and Qualification program and provides leadership and mentorship in the qualification of equipment, utilities, and processes. · ...

SOKOL GxP Services is seeking an experienced and detail-oriented Validation Engineer to support temperature and environmental mapping activities for GMP-controlled spaces, equipment, and utilities. · ...

Validation Engineer - Sterile Manufacturing · Fairless Hills, PA · $85,000 - $100,000 · Bonus Eligible (company performance based), 1st Shift, High-Impact GMP Role · Are you ready to join a sterile manufacturing site entering active production and play a direct role in qualifying ...

This role will provide YOU the opportunity to lead key activities to progress YOUR career. · ...

Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. · ...

SOKOL GxP Services is seeking an experienced and detail-oriented Validation Engineer to support temperature and environmental mapping activities for GMP-controlled spaces, equipment, and utilities. · ...

The ideal candidate is a recent engineering graduate with an interest in automation and control systems used in life sciences manufacturing (vaccines, biologics, cell and gene therapy). · Recent college degree in engineering with an interest in control systems testing. · Prefera ...

We are looking for professionals with the required skills to achieve our goals: · Bachelor's degree in Mechanical, Electrical or Chemical Engineering, or BS/BA in a related scientific discipline (e.g. Chemistry, Biology). · 5+ years of relevant technical experience in a validati ...